Evidence map›Paper›PMID 29176677›Full record

ArticleScientific reports2017

Organoids model distinct Vitamin E effects at different stages of prostate cancer evolution.

Rose N Njoroge, Kenji Unno, Jonathan C Zhao, Anum F Naseem, Jonathan F Anker, Warren A McGee, Larisa Nonn, Sarki A Abdulkadir

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. The Use of Organoid Cultures in Advancing Nutrition Research.Advances in nutrition (Bethesda, Md.) · 2025
    Review
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  15. Organoids Increase the Predictive Value ofFrontiers in oncology · 2019
    Article
  16. Vitamin E - a cause for concern?Clinical medicine (London, England) · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Rose N NjorogeNorthwestern University, Feinberg School of Medicine, Department of Urology, Chicago, IL, 60611, USA.
Kenji UnnoNorthwestern University, Feinberg School of Medicine, Department of Urology, Chicago, IL, 60611, USA.
Jonathan C ZhaoDivision of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Anum F NaseemNorthwestern University, Feinberg School of Medicine, Department of Urology, Chicago, IL, 60611, USA.
Jonathan F AnkerNorthwestern University, Feinberg School of Medicine, Department of Urology, Chicago, IL, 60611, USA.
Warren A McGeeDepartment of Neurology, Northwestern University, Chicago, IL, USA.
Larisa NonnDepartment of Pathology, University of Illinois at Chicago, Chicago, IL, 60612, USA.
Sarki A AbdulkadirNorthwestern University, Feinberg School of Medicine, Department of Urology, Chicago, IL, 60611, USA. sarki.abdulkadir@northwestern.edu.
Northwestern University · USUniversity of Illinois Chicago · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008152 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARDEHALI, HOSSEIN · 1987 to 2021
$24.0M
Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A. · 2015 to 2025
$19.9M
Research Education CoreU54CA202997 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CIECIERSKI, CHRISTINA, FEINGLASS, JOSEPH M · 2015 to 2024
$13.8M
Research Education CoreU54CA203000 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CIECIERSKI, CHRISTINA, FEINGLASS, JOSEPH M · 2015 to 2024
$12.4M
The Chicago Cancer Health Equity Collaborative (ChicagoCHEC)U54CA202995 · NCI · NORTHEASTERN ILLINOIS UNIVERSITY · PI CIECIERSKI, CHRISTINA · 2015 to 2024
$9.5M
Medical Scientist Training ProgramT32GM144295 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ALAN R HAUSER · 2022 to 2026
$9.1M
Role of Oncogenic Kinase Pim-1 in Prostate CancerR01CA123484 · NCI · VANDERBILT UNIVERSITY · PI ABDULKADIR, SARKI A. · 2007 to 2017
$2.9M
Prostate Cancer Recurrence: models and mechanismsR01CA167966 · NCI · VANDERBILT UNIVERSITY · PI ABDULKADIR, SARKI A. · 2012 to 2016
$1.8M
Genomics and bioinformatics analysis to understand castration-resistant prostate cancerR50CA211271 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHAO, CHANGSHENG · 2016 to 2020
$701k
TDP-43-regulated microRNAs and TDP-43 ProteinopathyF30NS090893 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MCGEE, WARREN ALEXANDER · 2014 to 2019
$203k
NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA123484NCI NIH HHS R01 CA167966NCI NIH HHS R50 CA211271NCI NIH HHS U54 CA202995NCI NIH HHS U54 CA202997NCI NIH HHS U54 CA203000NIGMS NIH HHS T32 GM008152NIGMS NIH HHS T32 GM144295NINDS NIH HHS F30 NS090893
6 · The paper itself

Abstract

Vitamin E increased prostate cancer risk in the Selenium and Vitamin E Cancer Prevention Trial (SELECT) through unknown mechanisms while Selenium showed no efficacy. We determined the effects of the SELECT supplements on benign (primary), premalignant ( RWPE-1) and malignant (LNCaP) prostate epithelial organoids. While the supplements decreased proliferation and induced cell death in cancer organoids, they had no effect on the benign organoids. In contrast, Vitamin E enhanced cell proliferation and survival in the premalignant organoids in a manner that recapitulated the SELECT results. Indeed, while Vitamin E induced a pro-proliferative gene expression signature, Selenium alone or combined with Vitamin E produced an anti-proliferative signature. The premalignant organoids also displayed significant downregulation of glucose transporter and glycolytic gene expression pointing to metabolic alterations. Detached RWPE-1 cells had low ATP levels due to diminished glucose uptake and glycolysis which was rescued by Vitamin E through the activation of fatty acid oxidation (FAO). FAO inhibition abrogated the ATP rescue, diminished survival of the inner matrix detached cells, restoring the normal hollow lumen morphology in Vitamin E treated organoids. Organoid models therefore clarify the paradoxical findings from SELECT and demonstrate that Vitamin E promotes tumorigenesis in the early stages of prostate cancer evolution.

Indexed as

AntioxidantsCell ProliferationCells, CulturedComputational BiologyHigh-Throughput Nucleotide SequencingHumansMaleMicroarray AnalysisOrganoidsOxygen ConsumptionProstatic NeoplasmsReactive Oxygen SpeciesTissue Culture TechniquesVitamin EAntioxidantsReactive Oxygen SpeciesVitamin E

Identifiers

PMID29176677
PMCPMC5701195
OpenAlexW2768370947

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.